JPH11289979A - O/w emulsion - Google Patents
O/w emulsionInfo
- Publication number
- JPH11289979A JPH11289979A JP10213845A JP21384598A JPH11289979A JP H11289979 A JPH11289979 A JP H11289979A JP 10213845 A JP10213845 A JP 10213845A JP 21384598 A JP21384598 A JP 21384598A JP H11289979 A JPH11289979 A JP H11289979A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- weight
- water
- egg yolk
- emulsion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Seasonings (AREA)
- Edible Oils And Fats (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、水中油型乳化物、
詳しくは、マヨネーズ、タルタルソース、乳化型ドレッ
シング等の酸性水中油型乳化物、更に詳しくは、冷凍後
に解凍し、更に加熱しても水中油型乳化が安定な、凍結
解凍耐性と加熱耐性とを合わせ持つ酸性水中油型乳化物
に関する。The present invention relates to an oil-in-water emulsion,
More specifically, acidic oil-in-water emulsions such as mayonnaise, tartar sauce, emulsified dressing, etc., and more specifically, oil-in-water emulsions that are stable after freezing and thawing even when further heated, have freeze-thaw resistance and heat resistance. The present invention relates to an acidic oil-in-water type emulsion having a combination.
【0002】[0002]
【従来の技術】食品用の調味料として、油脂、卵黄や全
卵や卵白等の卵原料、食酢、調味料等を主原料として作
られたマヨネーズ、タルタルソース、乳化型ドレッシン
グ等の酸性水中油型乳化物があり、これらは外食、サラ
ダ他の惣菜、製菓、製パン業界等に広く使用されてい
る。ところで近年、食品の冷凍技術の進歩と電子レンジ
の普及により、多種多様な冷凍食品が開発され市販され
ている。これら冷凍食品の中には、冷凍フライの様に畜
肉や魚介類とマヨネーズ、タルタルソース、乳化型ドレ
ッシング等の調味料を食品に内包させた後に衣を付けて
冷凍したものや、あらかじめマヨネーズ、タルタルソー
ス、乳化型ドレッシング等の調味料を上掛けした後に冷
凍したものがある。これら食品は、冷凍状態のまま油で
揚げたり、オーブンで焼いたり、電子レンジで加熱する
だけで食することができ非常に便利である。2. Description of the Related Art As a seasoning for foods, oil-in-water oils such as mayonnaise, tartar sauce, emulsified dressing, etc. made mainly from oils and fats, egg ingredients such as egg yolk, whole eggs and egg whites, vinegar and seasonings. There are type emulsions, which are widely used in eating out, salads and other prepared foods, confectionery, baking industry and the like. By the way, in recent years, a variety of frozen foods have been developed and marketed due to the progress of food freezing technology and the spread of microwave ovens. Some of these frozen foods include meat and seafood and seasonings such as mayonnaise, tartar sauce, emulsified dressing, etc., as in frozen fried food, which are then put on clothes and frozen, or mayonnaise and tartar in advance. There are some which are seasoned with sauce, emulsified dressing or the like and then frozen. These foods are very convenient because they can be eaten only by frying in a frozen state, baking in an oven, or heating in a microwave oven.
【0003】しかし、普通のマヨネーズ、タルタルソー
ス、乳化型ドレッシング等の酸性水中油型乳化物では、
冷凍保管後の解凍の時の使用されている原材料、特に卵
原料の冷凍変性によるものと推定されるが水中油型乳化
安定性が不安定化したり、更に冷凍状態から一気に加熱
された時に水分の上昇や原材料の加熱変性によって水中
油型乳化が破壊される結果、油が分離し食品の外観、食
感、風味が著しく損なわれるという問題がある。特に電
子レンジでの加熱では、マイクロ波により数分で品温が
急激に上昇するため水分の蒸発が著しく、また加熱変性
も急激に起こるため、一層水中油型乳化が破壊され易い
という問題がある。[0003] However, in an acidic oil-in-water emulsion such as ordinary mayonnaise, tartar sauce, and emulsion dressing,
It is presumed that this is due to the freeze denaturation of the raw materials used during thawing after frozen storage, especially egg raw materials.However, the oil-in-water emulsion stability becomes unstable, and when heated from a frozen state at a stretch, the water content is reduced. The oil-in-water emulsification is destroyed by the rise or the heat denaturation of the raw materials, resulting in a problem that oil is separated and the appearance, texture and flavor of the food are significantly impaired. In particular, in the case of heating in a microwave oven, there is a problem that the temperature of the product rapidly rises in a few minutes due to the microwave, so that the evaporation of water is remarkable, and the heat denaturation also occurs rapidly, so that the oil-in-water emulsion is more easily destroyed. .
【0004】これらの問題を解決するための手段とし
て、各種の水中油型乳化物が提案されている。例えば、
ホスフォリパーゼAによって変性させたホスフォリポー
たん白質を加える方法(特公昭53−44426号公
報)、トリプシン処理した部分加水分解卵黄を用いて水
性原料と油性原料とを乳化させる方法(特公平5−47
186号公報)、油相原料の一部として極度硬化油を使
用する方法(特公昭62−25340号公報)等があ
る。[0004] As means for solving these problems, various oil-in-water emulsions have been proposed. For example,
A method of adding a phospholipase protein denatured by phospholipase A (Japanese Patent Publication No. 53-44426), a method of emulsifying an aqueous raw material and an oily raw material using trypsin-treated partially hydrolyzed egg yolk (Japanese Patent Publication No. 5-47)
186) and a method of using extremely hardened oil as a part of the oil phase raw material (Japanese Patent Publication No. 62-25340).
【0005】しかしながら、これらの方法にても冷凍期
間が数週間程度の短期間の場合には冷凍解凍耐性は良好
だが、冷凍期間が長くなる程、使用されている原料の経
日的な冷凍変性によるものと推定されるが水中油型乳化
安定性が不安定化し、冷凍解凍後に油の分離が生じる傾
向があった。更に引き続き加熱により水中油型乳化が著
しく破壊され油が分離してしまうため、冷凍解凍耐性及
び加熱耐性の両方を満足させるという点において、未だ
不十分であった。However, these methods also have good freeze-thaw resistance when the freezing period is as short as several weeks, but the longer the freezing period is, the longer the freezing and denaturation of the raw materials used are. However, the oil-in-water emulsion stability was destabilized, and the oil tended to separate after freezing and thawing. Furthermore, the oil-in-water emulsification is remarkably destroyed by the subsequent heating and the oil is separated, so that it is still insufficient in satisfying both the freeze-thaw resistance and the heat resistance.
【0006】[0006]
【発明が解決しようとする課題】従って、本発明の目的
は、比較的水分の割合が高い水中油型乳化物であって
も、冷凍期間の長い冷凍食品に使用しても冷凍解凍の際
に水中油型乳化が安定であり、更に引き続き加熱しても
水中油型乳化が安定で油の分離が起こらない水中油型乳
化物、特に、マヨネーズ、タルタルソース、乳化型ドレ
ッシング等の酸性水中油型乳化物を提供することにあ
る。Accordingly, an object of the present invention is to provide an oil-in-water type emulsion having a relatively high water content, even when used for frozen foods having a long freezing period, when frozen and thawed. Oil-in-water emulsions are stable, and oil-in-water emulsions are stable even if subsequently heated and oil separation does not occur, especially acidic oil-in-water emulsions such as mayonnaise, tartar sauce, and emulsion dressing It is to provide an emulsion.
【0007】[0007]
【課題を解決するための手段】本発明者らは、マヨネー
ズ、タルタルソース、乳化型ドレッシング等の酸性水中
油型乳化物に関する前述の問題点を解決すべく鋭意研究
検討を重ねた結果、特定の原材料を組み合わせることに
よって、上記目的を達成し得ることを知見した。Means for Solving the Problems The present inventors have conducted intensive studies and studies to solve the above-mentioned problems concerning acidic oil-in-water emulsions such as mayonnaise, tartar sauce, emulsified dressing and the like. It has been found that the above object can be achieved by combining raw materials.
【0008】本発明は、上記知見に基づきなされたもの
で、油相8〜50重量%、酵素処理卵黄1〜15重量%
及び水相20〜80重量%を含有することを特徴とする
水中油型乳化物を提供するものである。[0008] The present invention has been made based on the above findings, comprising 8 to 50% by weight of an oil phase and 1 to 15% by weight of an enzyme-treated egg yolk.
An oil-in-water emulsion characterized by containing 20 to 80% by weight of an aqueous phase.
【0009】[0009]
【発明の実施の形態】以下、本発明の水中油型乳化物に
ついて詳細に説明する。本発明で使用される油相として
は油脂が用いられ、該油脂としては、食用に適する油脂
であればよく、例えば、大豆油、菜種油、コーン油、綿
実油、オリーブ油、落花生油、米油、べに花油、ひまわ
り油等の常温で液体の油脂が一般的であるが、更にパー
ム油、パーム核油、ヤシ油、サル脂、マンゴ脂、乳脂等
の常温で固体の油脂も除外されるものではなく、更にこ
れらの硬化油、分別油、エステル交換油等の物理的また
は化学的処理を施した油脂を使用することができる。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the oil-in-water emulsion of the present invention will be described in detail. Fats and oils are used as the oil phase used in the present invention. The fats and oils may be any edible fats and oils, such as soybean oil, rapeseed oil, corn oil, cottonseed oil, olive oil, peanut oil, rice oil, and beniflower Oils and liquids at room temperature such as sunflower oil are common, but oils and fats that are solid at room temperature such as palm oil, palm kernel oil, coconut oil, monkey fat, mango fat, and milk fat are not excluded. Further, fats and oils which have been subjected to physical or chemical treatment such as hardened oil, fractionated oil, and transesterified oil can be used.
【0010】好ましい油相としては、炭素数20以上の
飽和脂肪酸1残基と不飽和脂肪酸2残基とからなるトリ
グリセリドを1.5重量%以上含有する油相であり、よ
り好ましくは炭素数20以上の飽和脂肪酸1残基と不飽
和脂肪酸2残基とからなるトリグリセリドを3重量%以
上含有する油相である。本発明でいう炭素数20以上の
飽和脂肪酸としては、アラキン酸、ベヘン酸、リグノセ
リン酸などがあげられる。また、不飽和脂肪酸として
は、オレイン酸、リノール酸、リノレン酸などがあげら
れるが特に制限はない。炭素数20以上の飽和脂肪酸残
基の結合位置は、トリグリセリドの1位、2位、3位の
いずれでもよい。A preferred oil phase is an oil phase containing 1.5% by weight or more of a triglyceride comprising one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid, and more preferably 20% or more. An oil phase containing 3% by weight or more of a triglyceride composed of one residue of a saturated fatty acid and two residues of an unsaturated fatty acid. Examples of the saturated fatty acid having 20 or more carbon atoms in the present invention include arachiic acid, behenic acid, lignoceric acid and the like. Examples of the unsaturated fatty acid include oleic acid, linoleic acid and linolenic acid, but are not particularly limited. The binding position of the saturated fatty acid residue having 20 or more carbon atoms may be any of the first, second, and third positions of triglyceride.
【0011】例えば、油相が通常マヨネーズ類やドレッ
シング類に使用されるサラダ油では、冷凍の際に水相が
凝固し容積が膨張することによって液体状体の油相が圧
迫され変形し、お互いに凝集してしまうため、解凍時に
油相が分離し易い。これに対し、油相に炭素数20以上
の飽和脂肪酸1残基と不飽和脂肪酸2残基とからなるト
リグリセリドを配合することにより、冷凍の際に油相は
微細な結晶となり、水相が凝固し膨張しても油相は微細
な結晶のまま保持され、変形することがないため、これ
を解凍した場合にも、油相は融解するだけであり、乳化
が破壊されることはない。For example, in a salad oil whose oil phase is usually used for mayonnaise and dressings, the water phase solidifies during freezing and expands in volume, so that the liquid oil phase is pressed and deformed. Because of aggregation, the oil phase is easily separated during thawing. On the other hand, when the oil phase is mixed with a triglyceride comprising one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid, the oil phase becomes fine crystals during freezing, and the water phase solidifies. Even if the oil phase expands, the oil phase is kept as fine crystals and does not deform. Therefore, when the oil phase is thawed, the oil phase only melts and the emulsification is not destroyed.
【0012】上記の好ましい油相を形成する上記トリグ
リセリドを1.5重量%以上含有する油脂を得るには、
菜種油、落花生油、魚油、サル脂、からし油、マンゴ脂
を分別してその低融点部分を使用するか、またはこれら
の油脂をエステル交換するか、或いは合成により得るこ
とができる。上記のような方法により炭素数20以上の
飽和脂肪酸1残基と不飽和脂肪酸2残基とからなるトリ
グリセリドを1.5重量%以上含有する油脂が得られる
のであり、菜種油、落花生油、魚油、サル脂、からし
油、マンゴー脂などの油脂そのものには、炭素数20以
上の飽和脂肪酸1残基と不飽和脂肪酸2残基とからなる
トリグリセリドは、1.1重量%程度して含まれていな
いため、天然の油脂をそのまま使用することはできな
い。In order to obtain an oil or fat containing 1.5% by weight or more of the above triglyceride which forms the above preferable oil phase,
It can be obtained by separating rapeseed oil, peanut oil, fish oil, monkey fat, mustard oil, mango fat and using the low melting point portion, or transesterifying these fats or oils, or by synthesis. By the method as described above, fats and oils containing 1.5% by weight or more of triglyceride composed of one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid can be obtained, and rapeseed oil, peanut oil, fish oil, Fats and oils such as monkey fat, mustard oil and mango fat contain about 1.1% by weight of a triglyceride comprising one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid. Therefore, natural fats and oils cannot be used as they are.
【0013】本発明における油相として、炭素数20以
上の飽和脂肪酸1残基と不飽和脂肪酸2残基とからなる
トリグリセリドを1.5重量%以上含有する油相を用い
る場合には、上記のような方法で得られた炭素数20以
上の飽和脂肪酸1残基と不飽和脂肪酸2残基とからなる
トリグリセリドを1.5重量%以上含有する油脂を1種
または2種以上混合して油相としてもよいし、さらに他
の食用油脂と混合して、混合油が炭素数20以上の飽和
脂肪酸1残基と不飽和脂肪酸2残基とからなるトリグリ
セリドを1.5重量%以上含有しているようにしてもよ
い。また、油相には、トコフェロール等の酸化防止剤
や、βカロチン等の着色剤の如き油脂に溶解する成分や
添加剤を加えてよい。When the oil phase containing 1.5% by weight or more of triglyceride composed of one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid is used as the oil phase in the present invention, One or more fats or oils containing 1.5% by weight or more of a triglyceride comprising one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid obtained by the above method are mixed together to form an oil phase. Or mixed with other edible fats and oils, and the mixed oil contains 1.5% by weight or more of triglyceride composed of one residue of a saturated fatty acid having 20 or more carbon atoms and two residues of an unsaturated fatty acid. You may do so. In addition, components or additives soluble in fats and oils such as an antioxidant such as tocopherol and a coloring agent such as β-carotene may be added to the oil phase.
【0014】上記油相の配合割合は、水中油型乳化の安
定化と、風味や食感を良くするために8〜50重量%で
あり、好ましくは15〜40重量%である。油相の配合
割合が50重量%より大きいと水中油型乳化が不安定化
し、また8重量%より小さいと得られる水中油型乳化
物、特に酸性水中油型乳化物の食感が悪くなる。The mixing ratio of the above oil phase is from 8 to 50% by weight, preferably from 15 to 40% by weight, in order to stabilize the oil-in-water emulsification and to improve the flavor and texture. When the blending ratio of the oil phase is more than 50% by weight, the oil-in-water emulsion becomes unstable, and when it is less than 8% by weight, the texture of the obtained oil-in-water emulsion, particularly the acidic oil-in-water emulsion becomes poor.
【0015】次に、本発明では、乳化剤として酵素で処
理した卵黄を使用する。酵素で処理しない卵黄を用いる
と、得られる水中油型乳化物、特に酸性水中油型乳化物
の冷凍解凍耐性、加熱耐性は劣ったものとなる。酵素処
理卵黄は、基質としては生卵黄、殺菌卵黄、加塩卵黄、
加糖卵黄のいずれも使用することができるが、得られる
水中油型乳化物の風味や、酵素反応時の微生物の増殖を
抑えることを考慮すると加塩卵黄が適しており、例えば
食塩が3〜20重量%添加された加塩卵黄を用いるのが
好ましく、更に好ましくは食塩が5〜8重量%添加され
た加塩卵黄を用いるのが良い。Next, in the present invention, egg yolk treated with an enzyme is used as an emulsifier. When an egg yolk not treated with an enzyme is used, the resulting oil-in-water emulsion, particularly an acidic oil-in-water emulsion, has poor freeze-thaw resistance and heat resistance. Enzyme-treated yolks include raw yolk, sterilized yolk, salted yolk,
Any of sweetened egg yolks can be used, but salted egg yolk is suitable in consideration of the flavor of the resulting oil-in-water emulsion and suppressing the growth of microorganisms during the enzymatic reaction. % Salted egg yolk is preferably used, and more preferably salted egg yolk added with 5 to 8% by weight of salt.
【0016】本発明で、酵素処理の際に用いる酵素とし
ては、ホスフォリパーゼA及びプロテアーゼの併用が好
ましい。ホスフォリパーゼAは、リン脂質加水分解酵素
とも呼ばれ、リン脂質をリゾリン脂質に分解する反応を
触媒する酵素であり、作用するエステル結合の位置の違
いにより、ホスフォリパーゼA1 (EC3.1.1.3
2)及びホスフォリパーゼA2 (EC3.1.1.4)
の2種類を使用することができ、豚等の哺乳類の膵液
や、微生物を起源とした市販のホスフォリパーゼAを使
用することができる。また、プロテアーゼとは、蛋白質
を加水分解する反応を触媒する酵素であり、植物、動
物、微生物を起源とした酵素、例えばパイナップルを起
源としたブロメライン、パパイヤを起源としたパパイ
ン、哺乳類の膵液を起源としたトリプシン、哺乳類の胃
液を起源としたペプシン、カビ由来のプロテアーゼ等、
市販のプロテアーゼを使用することができ、特にブロメ
ラインが最適である。In the present invention, the enzyme used in the enzyme treatment is preferably a combination of phospholipase A and a protease. Phospholipase A is also called a phospholipid hydrolase and is an enzyme that catalyzes a reaction for decomposing phospholipids into lysophospholipids. Phospholipase A 1 (EC3.1) depends on the position of an acting ester bond. .1.3
2) and phospholipase A 2 (EC 3.1.1.4)
And pancreatic juice of mammals such as pigs, and commercially available phospholipase A derived from microorganisms can be used. Proteases are enzymes that catalyze the reaction of hydrolyzing proteins, and are enzymes derived from plants, animals and microorganisms, such as bromelain derived from pineapple, papain derived from papaya, and pancreatic fluid derived from mammals. Trypsin, pepsin derived from mammalian gastric juice, mold-derived protease, etc.
Commercially available proteases can be used, especially bromelain.
【0017】卵黄の酵素処理の際、ホスフォリパーゼA
及びプロテアーゼの添加は任意の順序、または同時に行
うことができるが、プロテアーゼによるホスホリパーゼ
Aの加水分解を避けるためには、卵黄をホスフォリパー
ゼAによる酵素処理後、プロテアーゼにより酵素処理す
るのが好ましい。When the yolk is enzymatically treated, phospholipase A
The addition of the protease and the protease can be performed in any order or at the same time, but in order to avoid the hydrolysis of phospholipase A by the protease, it is preferable that the egg yolk is subjected to the enzyme treatment with the phospholipase A and then the enzyme treatment with the protease.
【0018】これらの酵素としては、市販されている食
品用の、粉末または液体の酵素を使用することができ
る。As these enzymes, commercially available powdery or liquid enzymes for food can be used.
【0019】ホスフォリパーゼAの添加量は、卵黄1g
に対し、好ましくは0.2〜100ホスフォリパーゼユ
ニット、更に好ましくは0.5〜20ホスフォリパーゼ
ユニットの活性量に相当する量を作用させるのがよい。
ホスフォリパーゼユニットとは、ホスフォリパーゼの活
性量をあらわす単位であり、1ホスフォリパーゼユニッ
トとは、pH8.0、40℃で卵黄にホスフォリパーゼ
Aを作用させたときに、卵黄中にリン脂質から1分間に
1マイクロモルの脂肪酸を遊離する活性量である。プロ
テアーゼの添加量は、卵黄1gに対し、好ましくは0.
01〜10プロテアーゼユニット、更に好ましくは0.
1〜5プロテアーゼユニットの活性量に相当する量を作
用させるのがよい。プロテアーゼユニットとは、pH
7.0、37℃でミルクカゼインにプロテアーゼを作用
させたときに、1分間に1マイクロモルのチロシンに相
当する呈色度を示す活性量である。The amount of phospholipase A added was 1 g of egg yolk.
However, it is preferable that an amount corresponding to the activity of 0.2 to 100 phospholipase units, more preferably 0.5 to 20 phospholipase units, is applied.
The phospholipase unit is a unit indicating the amount of phospholipase activity, and one phospholipase unit is expressed in the yolk when phospholipase A is allowed to act on the yolk at pH 8.0 and 40 ° C. It is the amount of activity that releases 1 micromole of fatty acids per minute from phospholipids. The amount of the protease added is preferably 0.1 to 1 g of egg yolk.
01 to 10 protease units, more preferably 0.1 to 10 protease units.
It is preferable to apply an amount corresponding to the activity amount of 1 to 5 protease units. Protease unit is pH
It is an activity amount showing a color degree corresponding to 1 micromol of tyrosine per minute when a protease is allowed to act on milk casein at 7.0 and 37 ° C.
【0020】尚、ホスフォリパーゼA及びプロテアーゼ
の併用からなる上記酵素は、次のような基準で添加して
も良い。即ち、上記酵素の添加量(合計量)は、卵黄1
00重量部に対し、好ましくは0.001〜0.8重量
部であり、更に好ましくは0.01〜0.3重量部であ
る。このとき、ホスフォリパーゼAとプロテアーゼとの
重量比は、好ましくは20/80〜90/10であり、
更に好ましくは40/60〜85/15である。The above enzyme comprising a combination of phospholipase A and a protease may be added according to the following criteria. That is, the addition amount (total amount) of the enzyme is 1 egg yolk.
The amount is preferably 0.001 to 0.8 parts by weight, more preferably 0.01 to 0.3 parts by weight, based on 00 parts by weight. At this time, the weight ratio of phospholipase A to protease is preferably 20/80 to 90/10,
More preferably, it is 40/60 to 85/15.
【0021】卵黄の酵素処理は、卵黄の蛋白質やホスフ
ォリパーゼA及びプロテアーゼが熱により変性せず、ホ
スフォリパーゼA及びプロテアーゼの最適温度で行うの
が良く、通常20〜60℃、更に好ましくは40〜55
℃の温度範囲で行うのが良い。また、酵素処理中に撹拌
機等で撹拌を行うのが有利である。また、卵黄の酵素処
理の際の反応時間に特に制約はないが、1〜30時間の
範囲内で行うのが好ましい。なお、卵黄を酵素処理する
方法としては、回分式で上述の条件により加水分解する
方法が採用されるが、連続式で加水分解する方法でもよ
い。The enzyme treatment of egg yolk is preferably carried out at an optimum temperature of phospholipase A and protease, without denaturation of the protein, phospholipase A and protease of the egg yolk by heat, and is usually 20 to 60 ° C., more preferably 20 to 60 ° C. 40-55
It is good to perform in the temperature range of ° C. Further, it is advantageous to carry out stirring with a stirrer or the like during the enzyme treatment. The reaction time for the enzyme treatment of egg yolk is not particularly limited, but it is preferable to carry out the reaction within the range of 1 to 30 hours. In addition, as a method of enzymatic treatment of egg yolk, a method of hydrolyzing in a batch system under the above-described conditions is adopted, but a method of hydrolyzing in a continuous system may be used.
【0022】卵黄の酵素処理の際に、ホスフォリパーゼ
A及びプロテアーゼの至適pHに調整するのが良く、こ
の目的のpH調整剤は食品用であれば特に限定されず、
例えば乳酸、クエン酸、グルコン酸、アジピン酸、コハ
ク酸、酒石酸、フマル酸、リンゴ酸、リン酸、アスコル
ビン酸、酢酸等の酸味料や、リン酸二水素ナトリウム、
リン酸二水素カリウム、食酢、果汁、発酵乳等の酸性物
質や、水酸化ナトリウム、水酸化カリウム、水酸化カル
シウム、クエン酸ナトリウム、酢酸ナトリウム、リン酸
水素二ナトリウム、リン酸水素二カリウム、リン酸三ナ
トリウム、アスコルビン酸ナトリウム等を用いることが
でき、例えばpH6〜9の範囲で行うのが好ましい。ま
た、卵黄の酵素処理の際に、酵素の安定剤として食品用
の塩化カルシウム、リン酸二水素カルシウム等のカルシ
ウム塩を添加しても良い。It is preferable to adjust the pH of the phospholipase A and the protease to the optimal pH during the enzyme treatment of the egg yolk. The pH adjuster for this purpose is not particularly limited as long as it is for food.
For example, acidulants such as lactic acid, citric acid, gluconic acid, adipic acid, succinic acid, tartaric acid, fumaric acid, malic acid, phosphoric acid, ascorbic acid, acetic acid, and sodium dihydrogen phosphate,
Acidic substances such as potassium dihydrogen phosphate, vinegar, fruit juice, fermented milk, sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium citrate, sodium acetate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, phosphorus Trisodium acid, sodium ascorbate and the like can be used, and for example, it is preferably carried out in a pH range of 6 to 9. In addition, during the enzyme treatment of egg yolk, a calcium salt such as calcium chloride for food and calcium dihydrogen phosphate may be added as a stabilizer for the enzyme.
【0023】ホスフォリパーゼAによる卵黄のリン脂質
のリゾリン脂質への分解の程度と、プロテアーゼによる
卵黄の蛋白質の加水分解の程度は、酵素の添加量、反応
温度、反応開始時のpH、酵素の安定剤の有無、反応時
間等の影響を受けるが、特に限定されない。例えば、ホ
スフォリパーゼAによる卵黄のリン脂質のリゾリン脂質
への分解の程度は卵黄に含まれる全リン脂質の30〜1
00重量%がリゾリン脂質に分解される程度までに分解
するのが好ましく、またプロテアーゼによる卵黄の蛋白
質の加水分解の程度は卵黄に含まれる蛋白質の加熱凝固
性が完全に失われる程度までに分解するのが好ましい。The degree of degradation of the yolk phospholipids into lysophospholipids by phospholipase A and the degree of hydrolysis of egg yolk proteins by proteases depend on the amount of enzyme added, reaction temperature, pH at the start of the reaction, It is affected by the presence or absence of the stabilizer, the reaction time, etc., but is not particularly limited. For example, the degree of decomposition of the phospholipid of egg yolk into lysophospholipid by phospholipase A is 30 to 1 of the total phospholipid contained in egg yolk.
Preferably, the protein is degraded to an extent that 00% by weight is decomposed into lysophospholipid, and the degree of hydrolysis of the protein of the yolk by the protease is degraded to such an extent that the protein contained in the yolk is completely lost to heat coagulation. Is preferred.
【0024】上記の酵素処理卵黄の配合割合は、水中油
型乳化の安定化と、風味や食感を良くするために1〜1
5重量%であり、好ましくは3〜12重量%である。酵
素処理卵黄の配合割合が15重量%より大きいと得られ
る水中油型乳化物、特に酸性水中油型乳化物の粘度が著
しく上昇し、また1重量%より小さいと水中油型乳化が
不安定である。The mixing ratio of the above-mentioned enzyme-treated egg yolk is from 1 to 1 in order to stabilize oil-in-water emulsification and to improve flavor and texture.
It is 5% by weight, preferably 3 to 12% by weight. When the blending ratio of the enzyme-treated egg yolk is more than 15% by weight, the viscosity of the obtained oil-in-water emulsion, particularly the acidic oil-in-water emulsion is significantly increased, and when it is less than 1% by weight, the oil-in-water emulsion becomes unstable. is there.
【0025】本発明の水中油型乳化物において、水相の
配合割合は20〜80重量%、好ましくは50〜70重
量%である。本発明の水中油型乳化物は、このように水
相の割合が高い状態でも安定で、冷凍解凍耐性と耐熱性
に優れたもので、特に酸性水中油型乳化物として好適で
ある。なお、本発明の水中油型乳化物を調製する際に、
上記水相は、前記酵素処理卵黄も含めて調製されるが、
このときの酵素処理卵黄は、上記水相の配合割合には含
めないものとする。In the oil-in-water emulsion of the present invention, the mixing ratio of the aqueous phase is 20 to 80% by weight, preferably 50 to 70% by weight. The oil-in-water emulsion of the present invention is stable even in such a state where the ratio of the aqueous phase is high, and has excellent freeze-thaw resistance and heat resistance, and is particularly suitable as an acidic oil-in-water emulsion. In preparing the oil-in-water emulsion of the present invention,
The aqueous phase is prepared including the enzyme-treated egg yolk,
The enzyme-treated egg yolk at this time is not included in the mixing ratio of the aqueous phase.
【0026】従って、本発明における水相には、通常マ
ヨネーズ、タルタルソース、乳化型ドレッシング等の酸
性水中油型乳化物に使用されている酸味料、増粘安定
剤、化工澱粉、調味料、香辛料、香料、食塩、糖類、デ
キストリン、乳蛋白質、着色料等の副原料を本発明の目
的を損なわない限り、任意に使用することができる。例
えば酸味料としては乳酸、クエン酸、グルコン酸、アジ
ピン酸、コハク酸、酒石酸、フマル酸、リンゴ酸、アス
コルビン酸、食酢、果汁、発酵乳等が挙げられ、増粘安
定剤としてはキサンタンガム、アルギン酸ナトリウム、
グアーガム、タラガントガム、ローカストビーンガム、
ジェランガム、ゼラチン、微小繊維状セルロース等が挙
げられ、化工澱粉としては、コーン、ワキシーコーン、
タピオカ、馬鈴薯、甘薯、小麦、米等の澱粉を起源と
し、この澱粉をアミラーゼ等の酵素で処理したものや、
酸やアルカリ、エステル化、リン酸架橋化、加熱、湿熱
処理等の物理的、化学的処理を行ったものが挙げられ、
更にこれら化工澱粉を、水に溶解し易い様にあらかじめ
加熱処理により糊化させたものが挙げられる。Therefore, the aqueous phase in the present invention contains acidulants, thickening stabilizers, modified starches, modified starches, seasonings, and spices which are usually used in acidic oil-in-water emulsions such as mayonnaise, tartar sauce, emulsified dressing and the like. Auxiliary materials such as perfumes, salt, sugars, dextrin, milk protein, coloring agents and the like can be arbitrarily used as long as the object of the present invention is not impaired. For example, acidulants include lactic acid, citric acid, gluconic acid, adipic acid, succinic acid, tartaric acid, fumaric acid, malic acid, ascorbic acid, vinegar, fruit juice, fermented milk and the like, and as a thickening stabilizer xanthan gum, alginic acid sodium,
Guar gum, tarragant gum, locust bean gum,
Gellan gum, gelatin, microfibrous cellulose and the like, as modified starch, corn, waxy corn,
Tapioca, potato, sweet potato, wheat, rice, etc. originated from starch and treated with enzymes such as amylase,
Acid and alkali, esterification, phosphoric acid cross-linking, heating, such as those subjected to physical and chemical treatments such as heat and moisture,
Further, there may be mentioned those obtained by preliminarily gelatinizing these modified starches by heat treatment so as to be easily dissolved in water.
【0027】本発明の水中油型乳化物は、例えば以下の
様にして得ることができる。まず、水に酵素処理卵黄、
食酢等の酸味料、食塩、水飴等の糖類、コショウ等の香
辛料を分散溶解させたものを水相とし、また大豆油に化
工澱粉、増粘安定剤を分散させたものを油相とする。次
いで、水相を撹拌しつつ油相を加え、水中油型予備乳化
物を得る。これをコロイドミル等の乳化機、ホモゲナイ
ザー等の均質化機で処理し仕上げ乳化を行い、本発明の
水中油型乳化物が得られる。The oil-in-water emulsion of the present invention can be obtained, for example, as follows. First, the enzyme-treated egg yolk in water,
An aqueous phase is prepared by dispersing and dissolving an acidulant such as vinegar, salt, sugar such as starch syrup, and a spice such as pepper. The aqueous phase is obtained by dispersing modified starch and a thickening stabilizer in soybean oil. Next, the oil phase is added while stirring the water phase to obtain an oil-in-water type pre-emulsion. This is treated with an emulsifier such as a colloid mill or a homogenizer such as a homogenizer to perform finish emulsification, whereby the oil-in-water emulsion of the present invention is obtained.
【0028】[0028]
【実施例】次に、実施例及び比較例を挙げ、本発明を更
に詳細に説明するが、これらは本発明を何ら制限するも
のではない。EXAMPLES Next, the present invention will be described in more detail with reference to Examples and Comparative Examples, which do not limit the present invention in any way.
【0029】〔実施例1〕食塩を7重量%含有した加塩
卵黄を水酸化ナトリウムにてpH8.5に調整し、この
もの100kgに対して豚の膵液由来のホスフォリパー
ゼAを600000ホスフォリパーゼユニット加え、4
5℃にて4時間処理し、次いでブロメライン20000
0ユニットを加え、45℃にて7時間反応させ、10℃
まで冷却し、酵素処理卵黄を得た。水31重量%、水飴
(水分30重量%)10重量%、食酢6重量%、食塩
1.8重量%、グルタミン酸ナトリウム0.2重量%、
上記酵素処理卵黄10重量%を混合して水相を調製し
た。別に、大豆油40重量%、ワキシーコーンをリン酸
架橋後に糊化した化工澱粉1重量%を混合して油相を調
製した。次いで、水相を撹拌しつつ油相を加え、水中油
型予備乳化物を得、これをコロイドミルにて乳化し、本
発明の水中油型乳化物を得た。この水中油型乳化物10
0gをポリエチレン製の袋に密封して−20℃で凍結
し、2ヵ月後に室温で解凍した時の状態と、引き続いて
開封して高周波出力500Wの電子レンジで60秒間加
熱処理後の状態を調べた。その結果を下記表1に示す。Example 1 Salted egg yolk containing 7% by weight of salt was adjusted to pH 8.5 with sodium hydroxide, and 100,000 kg of the phospholipase A derived from porcine pancreatic juice was converted to 600,000 phospholipase. Unit plus 4
Treatment at 5 ° C. for 4 hours, then bromelain 20000
0 units were added, and reacted at 45 ° C for 7 hours.
The mixture was cooled to obtain an enzyme-treated egg yolk. Water 31% by weight, starch syrup (water 30% by weight) 10% by weight, vinegar 6% by weight, salt 1.8% by weight, sodium glutamate 0.2% by weight,
An aqueous phase was prepared by mixing 10% by weight of the enzyme-treated egg yolk. Separately, an oil phase was prepared by mixing 40% by weight of soybean oil and 1% by weight of modified starch obtained by gelatinizing waxy corn after phosphoric acid crosslinking. Next, the oil phase was added while stirring the aqueous phase to obtain an oil-in-water type pre-emulsion, which was emulsified by a colloid mill to obtain an oil-in-water type emulsion of the present invention. This oil-in-water emulsion 10
0 g was sealed in a polyethylene bag, frozen at -20 ° C and thawed at room temperature two months later, and subsequently opened and examined after heating in a microwave oven with high frequency output of 500 W for 60 seconds. Was. The results are shown in Table 1 below.
【0030】〔比較例1〕水31重量%、水飴(水分3
0重量%)10重量%、食酢6重量%、食塩1.8重量
%、グルタミン酸ナトリウム0.2重量%、7重量%加
塩卵黄10重量%を混合して水相を調製した。別に、大
豆油40重量%、ワキシーコーンをリン酸架橋後に糊化
した化工澱粉1重量%を混合して油相を調製した。次い
で、水相を撹拌しつつ油相を加え、水中油型予備乳化物
を得、これをコロイドミルにて乳化し、水中油型乳化物
を得た。この水中油型乳化物100gをポリエチレン製
の袋に密封して−20℃で凍結し、2ヵ月後に室温で解
凍した時の状態と、引き続いて開封して高周波出力50
0Wの電子レンジで60秒間加熱処理後の状態を調べ
た。その結果を下記表1に示す。Comparative Example 1 31% by weight of water, syrup (water 3
0% by weight), 10% by weight of vinegar, 1.8% by weight of salt, 0.2% by weight of sodium glutamate, 7% by weight, and 10% by weight of salted egg yolk were mixed to prepare an aqueous phase. Separately, an oil phase was prepared by mixing 40% by weight of soybean oil and 1% by weight of modified starch obtained by gelatinizing waxy corn after phosphoric acid crosslinking. Next, the oil phase was added while stirring the water phase to obtain an oil-in-water type pre-emulsion, which was emulsified by a colloid mill to obtain an oil-in-water type emulsion. 100 g of the oil-in-water emulsion was sealed in a polyethylene bag, frozen at −20 ° C., thawed at room temperature two months later, and then opened to obtain a high-frequency output of 50 μm.
The state after the heat treatment in a microwave oven of 0 W for 60 seconds was examined. The results are shown in Table 1 below.
【0031】〔実施例2〕水52.8重量%、水飴(水
分30重量%)12重量%、食酢7重量%、食塩1.8
重量%、グルタミン酸ナトリウム0.2重量%、荒挽き
胡椒0.2重量%、実施例1で使用したものと同じ酵素
処理卵黄8重量%を混合して水相を調製した。別に、菜
種サラダ油15重量%、ワキシーコーンをリン酸架橋後
に糊化した化工澱粉3重量%を混合して油相を調製し
た。次いで、水相を撹拌しつつ油相を加え、水中油型予
備乳化物を得、これをホモゲナイザーにて均質化し、本
発明の水中油型乳化物を得た。この水中油型乳化物10
0gをポリエチレン製の袋に密封して−20℃で凍結
し、2ヵ月後に室温で解凍した時の状態と、引き続いて
開封して高周波出力500Wの電子レンジで60秒間加
熱処理後の状態を調べた。その結果を下記表1に示す。Example 2 52.8% by weight of water, 12% by weight of syrup (30% by weight of water), 7% by weight of vinegar, 1.8% of salt
% Of sodium glutamate, 0.2% by weight of coarsely ground pepper, and 8% by weight of the same enzyme-treated egg yolk as used in Example 1 to prepare an aqueous phase. Separately, an oil phase was prepared by mixing 15% by weight of rapeseed salad oil and 3% by weight of modified starch obtained by gelatinizing waxy corn after crosslinking with phosphoric acid. Next, the oil phase was added while stirring the water phase to obtain an oil-in-water type pre-emulsion, which was homogenized with a homogenizer to obtain the oil-in-water type emulsion of the present invention. This oil-in-water emulsion 10
0 g was sealed in a polyethylene bag, frozen at -20 ° C and thawed at room temperature two months later, and subsequently opened and examined after heating in a microwave oven with high frequency output of 500 W for 60 seconds. Was. The results are shown in Table 1 below.
【0032】〔比較例2〕水52.8重量%、水飴(水
分30重量%)12重量%、食酢7重量%、食塩1.8
重量%、グルタミン酸ナトリウム0.2重量%、荒挽き
胡椒0.2重量%、7重量%加塩卵黄8重量%を混合し
て水相を調製した。別に、菜種サラダ油15重量%、ワ
キシーコーンをリン酸架橋後に糊化した化工澱粉3重量
%を混合して油相を調製した。次いで、水相を撹拌しつ
つ油相を加え、水中油型予備乳化物を得、これをホモゲ
ナイザーにて均質化し、本発明の水中油型乳化物を得
た。この水中油型乳化物100gをポリエチレン製の袋
に密封して−20℃で凍結し、2ヵ月後に室温で解凍し
た時の状態と、引き続いて開封して高周波出力500W
の電子レンジで60秒間加熱処理後の状態を調べた。そ
の結果を下記表1に示す。Comparative Example 2 52.8% by weight of water, 12% by weight of syrup (30% by weight of water), 7% by weight of vinegar, 1.8% of salt
An aqueous phase was prepared by mixing 0.2% by weight of sodium glutamate, 0.2% by weight of coarsely ground pepper and 8% by weight of salted egg yolk. Separately, an oil phase was prepared by mixing 15% by weight of rapeseed salad oil and 3% by weight of modified starch obtained by gelatinizing waxy corn after crosslinking with phosphoric acid. Next, the oil phase was added while stirring the water phase to obtain an oil-in-water type pre-emulsion, which was homogenized with a homogenizer to obtain the oil-in-water type emulsion of the present invention. 100 g of the oil-in-water emulsion was sealed in a polyethylene bag, frozen at −20 ° C., thawed at room temperature two months later, and subsequently opened and opened to obtain a high-frequency output of 500 W
The state after the heat treatment in the microwave oven for 60 seconds was examined. The results are shown in Table 1 below.
【0033】〔実施例3〕水23.8重量%、水飴(水
分30重量%)10重量%、食酢7重量%、食塩1.8
重量%、グルタミン酸ナトリウム0.2重量%、荒挽き
胡椒0.1重量%、タマゴフレーバー0.1重量%、実
施例1で使用したものと同じ酵素処理卵黄12重量%を
混合して水相を調製した。別に、菜種サラダ油45重量
%を油相とした。水相を撹拌しつつ油相を加え、水中油
型予備乳化物を得、これをホモゲナイザーにて均質化
し、本発明の水中油型乳化物を得た。この水中油型乳化
物100gをポリエチレン製の袋に密封して−20℃で
凍結し、2ヵ月後に室温で解凍した時の状態と、引き続
いて開封して高周波出力500Wの電子レンジで60秒
間加熱処理後の状態を調べた。その結果を下記表1に示
す。Example 3 23.8% by weight of water, 10% by weight of starch syrup (30% by weight of water), 7% by weight of vinegar, 1.8% of salt
% By weight, sodium glutamate 0.2% by weight, ground pepper 0.1% by weight, egg flavor 0.1% by weight, and the same enzyme-treated egg yolk 12% by weight as used in Example 1 were mixed to form an aqueous phase. Prepared. Separately, 45% by weight of rapeseed salad oil was used as the oil phase. While stirring the aqueous phase, the oil phase was added to obtain an oil-in-water type pre-emulsion, which was homogenized with a homogenizer to obtain the oil-in-water type emulsion of the present invention. 100 g of this oil-in-water emulsion was sealed in a polyethylene bag, frozen at -20 ° C, thawed at room temperature two months later, and then opened and heated in a microwave oven with high frequency output of 500 W for 60 seconds. The state after the treatment was examined. The results are shown in Table 1 below.
【0034】〔実施例4〕食塩を8重量%含有した加塩
卵黄を水酸化ナトリウムにてpH8.0に調整し、この
もの100kgに対して豚の膵液由来のホスフォリパー
ゼAを300000ホスフォリパーゼユニット加え、4
5℃にて5時間処理し、次いでブロメライン80000
ユニットを加え、45℃にて10時間反応させ、10℃
まで冷却し、酵素処理卵黄を得た。水23.8重量%、
水飴(水分30重量%)10重量%、食酢7重量%、食
塩1.8重量%、グルタミン酸ナトリウム0.2重量
%、荒挽き胡椒0.1重量%、タマゴフレーバー0.1
重量%、上記酵素処理卵黄12重量%を混合して水相を
調製した。別に、菜種サラダ油45重量%を油相とし
た。水相を撹拌しつつ油相を加え、水中油型予備乳化物
を得、これをホモゲナイザーにて均質化し、本発明の水
中油型乳化物を得た。この水中油型乳化物100gをポ
リエチレン製の袋に密封して−20℃で凍結し、2ヵ月
後に室温で解凍した時の状態と、引き続いて開封して高
周波出力500Wの電子レンジで60秒間加熱処理後の
状態を調べた。その結果を下記表1に示す。Example 4 A salted egg yolk containing 8% by weight of sodium chloride was adjusted to pH 8.0 with sodium hydroxide, and 100,000 of this was supplemented with 300,000 phospholipase A derived from porcine pancreatic juice. Unit plus 4
Treat at 5 ° C. for 5 hours, then bromelain 80000
Add the unit and react at 45 ° C for 10 hours.
The mixture was cooled to obtain an enzyme-treated egg yolk. 23.8% by weight of water,
10% by weight of starch syrup (30% by weight of water), 7% by weight of vinegar, 1.8% by weight of salt, 0.2% by weight of sodium glutamate, 0.1% by weight of ground pepper, 0.1% of egg flavor
By weight, 12% by weight of the above-mentioned enzyme-treated egg yolk was mixed to prepare an aqueous phase. Separately, 45% by weight of rapeseed salad oil was used as the oil phase. While stirring the aqueous phase, the oil phase was added to obtain an oil-in-water type pre-emulsion, which was homogenized with a homogenizer to obtain the oil-in-water type emulsion of the present invention. 100 g of this oil-in-water emulsion was sealed in a polyethylene bag, frozen at -20 ° C, thawed at room temperature two months later, and then opened and heated in a microwave oven with high frequency output of 500 W for 60 seconds. The state after the treatment was examined. The results are shown in Table 1 below.
【0035】〔実施例5〕水31重量%、水飴(水分3
0重量%)10重量%、食酢6重量%、食塩1.8重量
%、グルタミン酸ナトリウム0.2重量%、実施例1で
使用したものと同じ酵素処理卵黄10重量%を混合して
水相を調製した。別に、あらかじめ融解したサル脂の低
融点分別油(融点10℃、沃素価60、アラキン酸1残
基とオレイン酸2残基とからなるトリグリセリドをおよ
そ10重量%含む)10重量%と大豆油30重量%、ワ
キシーコーン澱粉をリン酸架橋後に糊化した化工澱粉1
重量%を混合して油相を調製した。次いで、水相を撹拌
しつつ油相を加え、水中油型予備乳化物を得、これをコ
ロイドミルにて乳化し、本発明の水中油型乳化物を得
た。この水中油型乳化物100gをポリエチレン製の袋
に密封して−20℃で凍結し、2ヵ月後に室温で解凍し
た時の状態と、引き続いて開封して高周波出力500W
の電子レンジで60秒間加熱処理後の状態を調べた。そ
の結果を下記表1に示す。Example 5 31% by weight of water, syrup (water 3
0% by weight) 10% by weight, 6% by weight of vinegar, 1.8% by weight of sodium chloride, 0.2% by weight of sodium glutamate, and 10% by weight of the same enzyme-treated egg yolk as used in Example 1 were mixed to form an aqueous phase. Prepared. Separately, 10% by weight of a pre-melted fractionated oil of low melting point of monkey fat (melting point 10 ° C., iodine value 60, containing about 10% by weight of triglyceride composed of one residue of arachiic acid and two residues of oleic acid) and 30% of soybean oil % By weight, modified starch obtained by gelatinizing waxy corn starch after crosslinking with phosphoric acid 1
The oil phase was prepared by mixing the weight%. Next, the oil phase was added while stirring the aqueous phase to obtain an oil-in-water type pre-emulsion, which was emulsified by a colloid mill to obtain an oil-in-water type emulsion of the present invention. 100 g of the oil-in-water emulsion was sealed in a polyethylene bag, frozen at −20 ° C., thawed at room temperature two months later, and subsequently opened and opened to obtain a high-frequency output of 500 W
The state after the heat treatment in the microwave oven for 60 seconds was examined. The results are shown in Table 1 below.
【0036】〔実施例6〕水23.8重量%、水飴(水
分30重量%)10重量%、食酢7重量%、食塩1.8
重量%、グルタミン酸ナトリウム0.2重量%、荒挽き
胡椒0.1重量%、タマゴフレーバー0.1重量%、実
施例4で使用したものと同じ酵素処理卵黄12重量%を
混合して水相を調製した。別に、ハイエルカ酸菜種油
(エルカ酸の割合が40重量%以上)の極度硬化油5重
量%と大豆サラダ油95重量%とのランダムエステル交
換油(ベヘン酸1残基と、オレイン酸、リノール酸、リ
ノレン酸のいずれかの不飽和脂肪酸2残基とからなるト
リグリセリドをおよそ33重量%含む)5重量%と菜種
サラダ油40重量%を混合して油相とした。次いで、水
相を撹拌しつつ油相を加え、水中油型予備乳化物を得、
これをコロイドミルにて乳化し、本発明の水中油型乳化
物を得た。この水中油型乳化物100gをポリエチレン
製の袋に密封して−20℃で凍結し、2ヵ月後に室温で
解凍した時の状態と、引き続いて開封して高周波出力5
00Wの電子レンジで60秒間加熱処理後の状態を調べ
た。その結果を下記表1に示す。Example 6 23.8% by weight of water, 10% by weight of starch syrup (30% by weight of water), 7% by weight of vinegar, 1.8% of salt
% By weight, 0.2% by weight of sodium glutamate, 0.1% by weight of coarsely ground pepper, 0.1% by weight of egg flavor, and 12% by weight of the same enzyme-treated egg yolk as used in Example 4 to form an aqueous phase. Prepared. Separately, random transesterification oil of 5% by weight of extremely hardened oil of high erucic acid rapeseed oil (the ratio of erucic acid is 40% by weight or more) and 95% by weight of soybean salad oil (one residue of behenic acid, oleic acid, linoleic acid, and linolenic acid) An oil phase was prepared by mixing 5% by weight of a triglyceride comprising 2 residues of any one of the unsaturated fatty acids of the acid) and 40% by weight of rapeseed salad oil. Next, the oil phase was added while stirring the water phase to obtain an oil-in-water type pre-emulsion,
This was emulsified in a colloid mill to obtain an oil-in-water emulsion of the present invention. 100 g of this oil-in-water emulsion was sealed in a polyethylene bag, frozen at -20 ° C., thawed at room temperature two months later, and then opened to obtain a high-frequency output of 5
The state after the heat treatment in a 00 W microwave oven for 60 seconds was examined. The results are shown in Table 1 below.
【0037】[0037]
【表1】 [Table 1]
【0038】〔実施例7〜10〕実施例1〜3で用いた
酵素処理卵黄に代えて、次のようにして得た酵素処理卵
黄を用いた以外は、実施例1〜3と同様にしてそれぞれ
本発明の水中油型乳化物を得た(それぞれ実施例7〜
9)。食塩を7重量%含有した加塩卵黄を水酸化ナトリ
ウムにてpH8.5に調整し、このもの100重量部に
対して豚の膵液由来のホスフォリパーゼAを0.01重
量部を加え、40℃にて7時間処理し、次いでブロメラ
イン0.002重量部を加え、45℃にて5時間反応さ
せ、10℃まで冷却し、酵素処理卵黄を得た。[Examples 7 to 10] In the same manner as in Examples 1 to 3, except that the enzyme-treated egg yolk obtained in the following manner was used instead of the enzyme-treated egg yolk used in Examples 1 to 3. Oil-in-water emulsions of the present invention were obtained (Examples 7 to 10).
9). A salted egg yolk containing 7% by weight of salt was adjusted to pH 8.5 with sodium hydroxide, and 0.01 part by weight of phospholipase A derived from porcine pancreatic juice was added to 100 parts by weight of the salted egg yolk. For 7 hours, and then added with 0.002 parts by weight of bromelain, reacted at 45 ° C. for 5 hours, and cooled to 10 ° C. to obtain enzyme-treated egg yolk.
【0039】また、実施例4で用いた酵素処理卵黄に代
えて、次のようにして得た酵素処理卵黄を用いた以外
は、実施例4と同様にして本発明の水中油型乳化物を得
た(実施例10)。食塩を8重量%含有した加塩卵黄を
水酸化ナトリウムにてpH8.0に調整し、このもの1
00重量部に対して豚の膵液由来のホスフォリパーゼA
を0.01重量部を加え、50℃にて3時間処理し、次
いでカビ由来のプロテアーゼ0.01重量部を加え、5
0℃にて3時間反応させ、10℃まで冷却し、酵素処理
卵黄を得た。The oil-in-water emulsion of the present invention was prepared in the same manner as in Example 4 except that the enzyme-treated egg yolk obtained in the following manner was used instead of the enzyme-treated egg yolk used in Example 4. (Example 10). A salted egg yolk containing 8% by weight of salt was adjusted to pH 8.0 with sodium hydroxide.
Phospholipase A derived from porcine pancreatic juice per 100 parts by weight
, And treated at 50 ° C. for 3 hours.
The mixture was reacted at 0 ° C. for 3 hours and cooled to 10 ° C. to obtain an enzyme-treated egg yolk.
【0040】実施例7〜10でそれぞれ得られた各水中
油型乳化物について、実施例1〜4と同様の評価を行っ
た結果、全く同様の効果が得られた。The oil-in-water emulsions obtained in Examples 7 to 10 were evaluated in the same manner as in Examples 1 to 4, and as a result, completely the same effects were obtained.
【0041】[0041]
【発明の効果】本発明の水中油型乳化物は、冷凍解凍耐
性と耐熱性を合わせもつ、特に酸性水中油型乳化物とし
て冷凍食品用途に好適なものである。本発明の水中油型
乳化物は、特に卵黄をホスフォリパーゼA及びプロテア
ーゼにより処理したものを原料として使用することによ
って、従来困難であった冷凍解凍状態から電子レンジ等
により一気に加熱された時でも、水中油型乳化が安定な
酸性水中油型乳化物を提供できる。The oil-in-water emulsion of the present invention has both freeze-thaw resistance and heat resistance, and is particularly suitable as an acidic oil-in-water emulsion for use in frozen foods. The oil-in-water emulsion of the present invention, particularly by using egg yolk treated with phospholipase A and protease as a raw material, even when heated at a stretch by a microwave oven or the like from a frozen and thawed state, which was conventionally difficult. In addition, an oil-in-water type emulsion having stable oil-in-water type emulsion can be provided.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 鈴木 隆 東京都荒川区東尾久7丁目2番35号 旭電 化工業株式会社内 ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Takashi Suzuki 7-35 Higashiogu, Arakawa-ku, Tokyo Asahi Denka Chemical Industry Co., Ltd.
Claims (6)
15重量%及び水相20〜80重量%を含有することを
特徴とする水中油型乳化物。1. Oil phase 8-50% by weight, enzyme-treated egg yolk 1
An oil-in-water emulsion comprising 15% by weight and 20 to 80% by weight of an aqueous phase.
A及びプロテアーゼで処理することにより得られた酵素
処理卵黄であることを特徴とする、請求項1に記載の水
中油型乳化物。2. The oil-in-water emulsion according to claim 1, wherein the enzyme-treated egg yolk is an enzyme-treated egg yolk obtained by treating egg yolk with phospholipase A and a protease.
Aで処理し、次いでプロテアーゼで処理することにより
得られた酵素処理卵黄であることを特徴とする、請求項
1又は2に記載の水中油型乳化物。3. The oil-in-water type according to claim 1, wherein the enzyme-treated egg yolk is an enzyme-treated egg yolk obtained by treating egg yolk with phospholipase A and then with protease. Emulsion.
とを特徴とする、請求項1〜3の何れかに記載の水中油
型乳化物。4. The oil-in-water emulsion according to claim 1, wherein the protease is bromelain.
残基と不飽和脂肪酸2残基とからなるトリグリセリドを
1.5重量%以上含有することを特徴とする、請求項1
〜4の何れかに記載の水中油型乳化物。5. The method according to claim 1, wherein the oil phase is a saturated fatty acid 1 having 20 or more carbon atoms.
The triglyceride comprising a residue and two unsaturated fatty acids is contained in an amount of 1.5% by weight or more.
5. The oil-in-water emulsion according to any one of items 1 to 4.
する、請求項1〜5の何れかに記載の水中油型乳化物。6. The oil-in-water emulsion according to claim 1, which is an acidic oil-in-water emulsion.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10213845A JPH11289979A (en) | 1998-02-13 | 1998-07-29 | O/w emulsion |
CNB991006844A CN1170485C (en) | 1998-02-13 | 1999-02-13 | Oil-in-water type emulsion liquid |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10-31774 | 1998-02-13 | ||
JP3177498 | 1998-02-13 | ||
JP10213845A JPH11289979A (en) | 1998-02-13 | 1998-07-29 | O/w emulsion |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH11289979A true JPH11289979A (en) | 1999-10-26 |
Family
ID=26370292
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10213845A Pending JPH11289979A (en) | 1998-02-13 | 1998-07-29 | O/w emulsion |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPH11289979A (en) |
CN (1) | CN1170485C (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100409766C (en) * | 2003-06-16 | 2008-08-13 | 花王株式会社 | Acidic oil-in-water type emulsion composition |
JP2009060856A (en) * | 2007-09-06 | 2009-03-26 | Kaneka Corp | Acid oil-in-water emulsified fat and oil composition |
EP2106706A1 (en) | 2008-03-31 | 2009-10-07 | Kraft Foods Global Brands LLC | A process and formulation for making an egg product with increased functionality and flavor |
JP2009284869A (en) * | 2008-05-30 | 2009-12-10 | Taiyo Yushi Kk | Oil-in-water emulsified oil-and-fat composition for whipped-cream |
CN102960774A (en) * | 2012-12-07 | 2013-03-13 | 北京二商健力食品科技有限公司 | Instant yolk powder and preparation method thereof |
CN102960772A (en) * | 2012-12-07 | 2013-03-13 | 北京二商健力食品科技有限公司 | Instant yolk powder and preparation method thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7662421B2 (en) * | 2002-03-18 | 2010-02-16 | Q.P. Corporation | Container-packed, oil-in-water type emulsified food product and method for manufacture thereof |
JP5101754B2 (en) * | 2011-01-31 | 2012-12-19 | 日清オイリオグループ株式会社 | Palm fractionated soft oil and processed emulsified food using the same |
Citations (4)
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---|---|---|---|---|
JPS6229950A (en) * | 1985-07-31 | 1987-02-07 | Q P Corp | Production of o/w-type emulsified food |
JPH08112075A (en) * | 1994-08-23 | 1996-05-07 | Asahi Denka Kogyo Kk | Acidic paste-state o/w-type emulsified oil and fat for salad |
JPH09121808A (en) * | 1995-11-06 | 1997-05-13 | Asahi Denka Kogyo Kk | Emulsifier produced by using yolk |
JPH09220065A (en) * | 1996-02-14 | 1997-08-26 | Kanegafuchi Chem Ind Co Ltd | Pasty oil-in-water type oil and fat emulsion composition |
-
1998
- 1998-07-29 JP JP10213845A patent/JPH11289979A/en active Pending
-
1999
- 1999-02-13 CN CNB991006844A patent/CN1170485C/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6229950A (en) * | 1985-07-31 | 1987-02-07 | Q P Corp | Production of o/w-type emulsified food |
JPH08112075A (en) * | 1994-08-23 | 1996-05-07 | Asahi Denka Kogyo Kk | Acidic paste-state o/w-type emulsified oil and fat for salad |
JPH09121808A (en) * | 1995-11-06 | 1997-05-13 | Asahi Denka Kogyo Kk | Emulsifier produced by using yolk |
JPH09220065A (en) * | 1996-02-14 | 1997-08-26 | Kanegafuchi Chem Ind Co Ltd | Pasty oil-in-water type oil and fat emulsion composition |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100409766C (en) * | 2003-06-16 | 2008-08-13 | 花王株式会社 | Acidic oil-in-water type emulsion composition |
JP2009060856A (en) * | 2007-09-06 | 2009-03-26 | Kaneka Corp | Acid oil-in-water emulsified fat and oil composition |
EP2106706A1 (en) | 2008-03-31 | 2009-10-07 | Kraft Foods Global Brands LLC | A process and formulation for making an egg product with increased functionality and flavor |
EP2517578A1 (en) | 2008-03-31 | 2012-10-31 | Kraft Foods Global Brands LLC | A process and formulation for making an egg product with increased functionality and flavor |
JP2009284869A (en) * | 2008-05-30 | 2009-12-10 | Taiyo Yushi Kk | Oil-in-water emulsified oil-and-fat composition for whipped-cream |
CN102960774A (en) * | 2012-12-07 | 2013-03-13 | 北京二商健力食品科技有限公司 | Instant yolk powder and preparation method thereof |
CN102960772A (en) * | 2012-12-07 | 2013-03-13 | 北京二商健力食品科技有限公司 | Instant yolk powder and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN1170485C (en) | 2004-10-13 |
CN1233416A (en) | 1999-11-03 |
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